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NCT07296952 · ClinicalTrials.gov registry record · NA

Using Implementation Science to Adapt a Targeted Transportation Intervention for Patients With Diabetic Retinopathy (PRONTO-EYE)

A NA study of Diabetic Retinopathy (DR), sponsored by University of Illinois at Chicago.

Recruiting
Registry status
NA
Development phase
60
Enrollment target
1
Study location

NCT07296952: Recruiting NA study of Diabetic Retinopathy (DR), sponsored by University of Illinois at Chicago.

NCT07296952 is a NA study of Diabetic Retinopathy (DR) that is actively recruiting participants, run by University of Illinois at Chicago. The registered enrollment target is 60 participants, below the 498-participant average among 5 other Diabetic Retinopathy (DR) trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07296952, a NA study of Diabetic Retinopathy (DR), is actively recruiting participants, sponsored by University of Illinois at Chicago.

RECRUITING
Registry status
NA
Development phase
60 participants
Enrollment target
1
Study location

Study Summary

This is a a type 3 hybrid effectiveness-implementation pilot study to evaluate the PRONTO-EYE intervention, a rideshare transportation program, in patients with diabetic retinopathy with Medicaid insurance on adherence to ophthalmology visits.

Primary Outcome

Proportion of patients who attend their scheduled ophthalmology visit compared to pre-implementation historical controls.

Conditions Studied

Interventions

  • BEHAVIORAL PRONTO-EYE

Study Locations (1)

Illinois

  • UI Health - Chicago

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2026-02-03
Est. Completion 2027-06-01
Phase NA
University of Illinois at Chicago

430 total trials

What NCT07296952 shows while recruiting

NCT07296952 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 498-participant average among 5 other Diabetic Retinopathy (DR) trials with a reported enrollment target (88% lower).

The record links to 1 condition, with Diabetic Retinopathy (DR) appearing as the primary indexed condition, and to 1 intervention - of which PRONTO-EYE is the first listed.

NCT07296952 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT07296952 about?

NCT07296952 is a clinical study titled "Using Implementation Science to Adapt a Targeted Transportation Intervention for Patients With Diabetic Retinopathy (PRONTO-EYE)". This is a a type 3 hybrid effectiveness-implementation pilot study to evaluate the PRONTO-EYE intervention, a rideshare transportation program, in patients with diabetic retinopathy with Medicaid insurance on adherence to ophthalmology visits.

What is the current status of trial NCT07296952?

This trial is currently recruiting. It is a NA study. The enrollment target is 60 participants. The study started on 2026-02-03. Estimated completion is 2027-06-01.

What conditions does trial NCT07296952 study?

This clinical trial studies the following conditions: Diabetic Retinopathy (DR).

What interventions are being tested in trial NCT07296952?

The interventions under investigation include: PRONTO-EYE (BEHAVIORAL).

Who is sponsoring clinical trial NCT07296952?

This trial is sponsored by University of Illinois at Chicago, which has 430 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07296952 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

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Source: ClinicalTrials.gov NCT07296952, the US trial registry maintained by the National Library of Medicine. NCT07296952 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.